Canonical Allele Identifier: CA2758363821

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529264_129529265insAGA , CM000665.2:g.129529264_129529265insAGA	GRCh38
NC_000003.11:g.129248107_129248108insAGA , CM000665.1:g.129248107_129248108insAGA	GRCh37
NC_000003.10:g.130730797_130730798insAGA	NCBI36
NG_009115.1:g.5626_5627insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+170_361+171insAGA MANE Select	ENSP00000296271.3:n.361+170_361+171insAGA
ENST00000296271.3:c.361+170_361+171insAGA	ENSP00000296271.3:n.361+170_361+171insAGA
NM_000539.3:c.361+170_361+171insAGA MANE Select	NP_000530.1:n.361+170_361+171insAGA